Rapid laboratory diagnosis of urinary tract infection, with or without antibiotic decision support-a small pilot study investigating accuracy and clinical impact.

IF 2.2 4区 医学 Q4 IMMUNOLOGY Apmis Pub Date : 2024-11-04 DOI:10.1111/apm.13491
Einar Nilsen, Kristine Karlsrud Berg, Fabian Åhrberg, Eivor Johanne Nordstrand Jacobsen, Kasper Kavli Øvstehus, Erik Otte
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Abstract

The study evaluated the accuracy and clinical impact of rapid diagnostics (RD) with or without antibiotic decision support (ADS) for hospitalized patients with urinary tract infections. A two-centre prospective intervention was conducted with 230 patients divided into three groups: RD-only (n = 59), RD plus ADS (n = 56) and a control group (n = 115). Mean laboratory turnaround time for RD was 10 h and 50 min. Of 115 microorganisms, 108 were correctly identified. The error rate for rapid susceptibility determination was 0.85%. Total antibiotic consumption, measured in defined daily doses (DDD), was lower in the intervention groups compared to the control group (ADS: 10.3 DDD, p = 0.01; RD: 10.9 DDD, p = 0.06; control: 13.0 DDD). No significant differences were observed in the use of broad-spectrum antibiotics (p = 0.816). Adherence to antibiotic guidelines was significantly better in the ADS group compared to the control group (p = 0.015) (RD vs control; p = 0.261). The ADS group also received fewer doses of ineffective antibiotics (ADS: 1.8 doses, p = 0.012; RD: 2.4 doses, p = 0.195; control: 3.4 doses). Length of hospital and ICU stays or 30-day readmission rates did not differ across groups. No in-hospital mortality was observed in any group.

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尿路感染的快速实验室诊断,有无抗生素决策支持--调查准确性和临床影响的小型试点研究。
这项研究评估了快速诊断(RD)与抗生素决策支持(ADS)对住院尿路感染患者的准确性和临床影响。研究人员在两个中心对 230 名患者进行了前瞻性干预,分为三组:仅使用 RD 组(59 人)、RD 加 ADS 组(56 人)和对照组(115 人)。RD 的平均实验室周转时间为 10 小时 50 分钟。在 115 种微生物中,108 种被正确鉴定。快速药敏测定的错误率为 0.85%。与对照组相比,干预组的抗生素总用量(以规定日剂量(DDD)计算)较低(ADS:10.3 DDD,p = 0.01;RD:10.9 DDD,p = 0.06;对照组:13.0 DDD)。广谱抗生素的使用没有明显差异(p = 0.816)。与对照组相比,ADS 组对抗生素指南的遵守情况明显更好(p = 0.015)(RD vs 对照组;p = 0.261)。ADS 组接受的无效抗生素剂量也更少(ADS:1.8 剂,p = 0.012;RD:2.4 剂,p = 0.195;对照组:3.4 剂)。各组的住院时间和重症监护室住院时间或 30 天再入院率没有差异。各组均未观察到院内死亡率。
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来源期刊
Apmis
Apmis 医学-病理学
CiteScore
5.20
自引率
0.00%
发文量
91
审稿时长
2 months
期刊介绍: APMIS, formerly Acta Pathologica, Microbiologica et Immunologica Scandinavica, has been published since 1924 by the Scandinavian Societies for Medical Microbiology and Pathology as a non-profit-making scientific journal.
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